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Title: Nonthermal Site Occupation at the Donor-Acceptor Interface of Organic Solar Cells

Journal Article · · Physical Review Applied
 [1];  [2];  [2];  [1]
  1. Pennsylvania State Univ., University Park, PA (United States)
  2. Princeton Univ., NJ (United States)

Here, we investigate the nature of occupation and relaxation within the charge transfer density of states (CT DOS) for bulk heterojunction organic solar cells consisting of the donor boron subphthalocyanine chloride and the acceptor C60. We observe relaxation of geminate CT states on a sub-ns timescale via an approximately 70-meV dynamic redshift in their photoluminescence, whereas free carrier relaxation at longer times leads to the formation of nongeminate CT states at even lower energy. In steady state, we find that thermalization within the DOS is incomplete, resulting in a Boltzmann-like CT state distribution characterized by an effective temperature above that of the ambient. These findings confirm that electron and hole populations can be far from equilibrium in organic solar cells and may prompt a reassessment of analyses that assume the same temperature for their charge-carrier distributions in the dark and under illumination.

Research Organization:
Princeton Univ., NJ (United States); Pennsylvania State Univ., University Park, PA (United States)
Sponsoring Organization:
USDOE Office of Science (SC), Basic Energy Sciences (BES)
Grant/Contract Number:
SC0012458; SC0012365
OSTI ID:
1595576
Alternate ID(s):
OSTI ID: 1546137
Journal Information:
Physical Review Applied, Vol. 10, Issue 3; ISSN 2331-7019
Publisher:
American Physical Society (APS)Copyright Statement
Country of Publication:
United States
Language:
English
Citation Metrics:
Cited by: 16 works
Citation information provided by
Web of Science

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Cited By (1)

Reply to: Triplet-triplet annihilation in rubrene/C60 OLEDs with electroluminescence turn-on breaking the thermodynamic limit journal October 2019